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Disease Ontology Browser
long QT syndrome 6 (DOID:0110648)
Alliance: disease page
Synonyms: LQT6
Alt IDs: OMIM:613693, ICD10CM:I45.8, MESH:C566333
Definition: A long QT interval syndrome that has_material_basis_in dominant inheritance of mutation in the KCNE2 gene on chromosome 21q22.11.


Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO)
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last database update
01/31/2023
MGI 6.22
The Jackson Laboratory